Sr. Validation Engineer @ Cardinal Health (January 2005 - December 2007)
Principal Validation Specialist @ ZLB Behring (Aventis Behring) (January 2000 - December 2005)
QA Manager @ Jordan Pharmaceuticals (January 1998 - December 2000)
Production Coordinator @ Wesley Jessen (Ciba) (January 1997 - December 1999)
Production Supervisor @ Solopak Pharmaceuticals (December 1992 - November 1997)
Mark Burger Education
Illinois State University 1987-1992
Mark Burger Skills
FDA
Computer System Validation
21 CFR Part 11
Validation
CAPA
Sop
Six Sigma
Aseptic Processing
GMP
V&V
Change Control
Biopharmaceuticals
Cleaning Validation
Quality Assurance
Microbiology
Regulatory Affairs
Quality System
Regulatory Requirements
HPLC
Quality Management
Contract Manufacturing
Pharmaceutical Industry
GAMP
Regulatory Submissions
Medical Devices
Quality Auditing
Drug Development
Biotechnology
Technology Transfer
GxP
GLP
Pharmaceutics
Quality Control
LIMS
ISO 13485
Analytical Chemistry
Chromatography
Design Control
Trackwise
Vaccines
R&D
Clinical Development
CRO
Program Management
Cross-functional Team Leadership
Manufacturing
Continuous Improvement
Process Improvement
Lean Manufacturing
Cross Functional Team Leadership
Computer System
Mark Burger Summary
Mark Burger, based in Chicago, IL, US, is currently a Sr. Manager, Small Molecule CoDev Lead at Pfizer. Mark Burger brings experience from previous roles at Hospira, a Pfizer Company, Active BioMaterial, Catalent Pharma Solutions and Cardinal Health/Catalent Pharma Solutions. Mark Burger holds a 1987 - 1992 Illinois State University. With a robust skill set that includes FDA, Computer System Validation, 21 CFR Part 11, Validation, CAPA and more. Mark Burger has 3 emails and 2 mobile phone numbers on RocketReach.
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